TY - JOUR
T1 - Post-Procedure Monocyte Count Levels Predict Major Adverse Cardiovascular Events (MACE) Following Transcatheter Aortic Valve Implantation (TAVI) for Aortic Stenosis
AU - Navani, Rohan V.
AU - Dayawansa, Nalin H.
AU - Nanayakkara, Shane
AU - Palmer, Sonny
AU - Noaman, Samer
AU - Htun, Nay M.
AU - Walton, Antony S.
AU - Peter, Karlheinz
AU - Stub, Dion
N1 - Funding Information:
Prof Stub\u2019s research is supported by an NHF and NHMRC Fellowship. Prof Peter is supported by an NHRMC Investigator Fellowship. Dr Dayawansa is supported by an Australian Commonwealth Government Research Training Program stipend and Baker Institute Bright Sparks Scholarship.
Funding Information:
The seminal study by Sinning et al. [12] demonstrated that lactate levels were elevated in those patients who developed a systemic inflammatory response syndrome post-TAVI compared to those who did not. Moreover, Sinning et al. [12] demonstrated a strong association between 30-day (18.0% vs 1.1%, p<0.001) and 1-year mortality (52.5% vs 9.9%, p<0.001) for those who developed systemic inflammatory response syndrome post-TAVI. The association between systemic inflammation induced by TAVI and subsequent adverse patient outcomes has been reported multiple times [ 20\u201323]. Thus, while it is known that there is an association between elevated monocyte counts and elevation of pro-inflammatory monocyte subsets and the severity of AS, the preprocedure monocyte count does not appear to predict the immune response to the TAVI procedure itself. This hypothesis is supported by the results of our study where preprocedure monocyte count did not correlate with 30-day MACE (OR 1.14, 95% CI 0.89\u20131.45; p=0.30).Prof Stub's research is supported by an National Heart Foundation and National Health and Research Council Fellowship. Prof Peter is supported by an NHRMC Investigator Fellowship. Dr Dayawansa is supported by an Australian Commonwealth Government Research Training Program stipend and Baker Institute Bright Sparks Scholarship, Australia.
Publisher Copyright:
© 2024 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ)
PY - 2024/9
Y1 - 2024/9
N2 - Background: Aortic stenosis has recently been characterised as having an inflammatory aetiology, beyond the traditional degenerative model. Recruitment of monocytes has been associated with inflammation contributing to progression of calcific aortic-valve disease. Prior research has demonstrated that pre-procedure inflammatory biomarkers do not consistently discriminate poorer outcomes in those with aortic stenosis. It remains, however, unclear if postprocedure inflammatory biomarkers, which are influenced by intraprocedural pro-inflammatory insults, can predict major adverse cardiovascular events (MACE) post transcatheter aortic valve implantation (TAVI). Method: All patients with postprocedure monocyte levels undergoing transcatheter aortic valve implantation at The Alfred Hospital, Melbourne, Australia (2008–2019) were included. The highest monocyte count from postprocedure days 1 to 3 was used. Patients were divided into “high” or “low” postprocedure monocyte count groups using the Youden Index. The incidence of 30-day MACE a composite of stroke, acute myocardial infarction, and death) was then compared. Results: In total, 472 patients were included (54% men, median age 84 years). Fourteen (14) patients (3%) suffered a 30-day MACE. Those with high postprocedure monocyte count were more likely to: be hypertensive (p=0.049); have a higher Society of Thoracic Surgeons risk score (p=0.032); and, undergo non-transfemoral access (p=0.018). A high (≥0.975) postprocedure monocyte count was significantly associated with 30-day MACE (odds ratio [OR] 1.16 for each 0.1 increase in monocyte, p=0.025). This association remained present on multivariable analysis adjusted for age, sex, Society of Thoracic Surgeons risk score, and self-expanding valve prosthesis type (OR 1.17, p=0.028). Conclusions: The association between postprocedure monocytosis and 30-day MACE suggests that minimising peri-procedural inflammatory insults may improve outcomes. This inexpensive and readily available biomarker may also aid in tailored risk stratification for patients.
AB - Background: Aortic stenosis has recently been characterised as having an inflammatory aetiology, beyond the traditional degenerative model. Recruitment of monocytes has been associated with inflammation contributing to progression of calcific aortic-valve disease. Prior research has demonstrated that pre-procedure inflammatory biomarkers do not consistently discriminate poorer outcomes in those with aortic stenosis. It remains, however, unclear if postprocedure inflammatory biomarkers, which are influenced by intraprocedural pro-inflammatory insults, can predict major adverse cardiovascular events (MACE) post transcatheter aortic valve implantation (TAVI). Method: All patients with postprocedure monocyte levels undergoing transcatheter aortic valve implantation at The Alfred Hospital, Melbourne, Australia (2008–2019) were included. The highest monocyte count from postprocedure days 1 to 3 was used. Patients were divided into “high” or “low” postprocedure monocyte count groups using the Youden Index. The incidence of 30-day MACE a composite of stroke, acute myocardial infarction, and death) was then compared. Results: In total, 472 patients were included (54% men, median age 84 years). Fourteen (14) patients (3%) suffered a 30-day MACE. Those with high postprocedure monocyte count were more likely to: be hypertensive (p=0.049); have a higher Society of Thoracic Surgeons risk score (p=0.032); and, undergo non-transfemoral access (p=0.018). A high (≥0.975) postprocedure monocyte count was significantly associated with 30-day MACE (odds ratio [OR] 1.16 for each 0.1 increase in monocyte, p=0.025). This association remained present on multivariable analysis adjusted for age, sex, Society of Thoracic Surgeons risk score, and self-expanding valve prosthesis type (OR 1.17, p=0.028). Conclusions: The association between postprocedure monocytosis and 30-day MACE suggests that minimising peri-procedural inflammatory insults may improve outcomes. This inexpensive and readily available biomarker may also aid in tailored risk stratification for patients.
KW - Aortic stenosis
KW - Biomarker
KW - Inflammation
KW - Monocyte count
KW - TAVI
UR - https://www.scopus.com/pages/publications/85195276749
U2 - 10.1016/j.hlc.2024.03.013
DO - 10.1016/j.hlc.2024.03.013
M3 - Article
C2 - 38845242
AN - SCOPUS:85195276749
SN - 1443-9506
VL - 33
SP - 1340
EP - 1347
JO - Heart Lung and Circulation
JF - Heart Lung and Circulation
IS - 9
ER -